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首页> 外文期刊>Journal of Endocrinological Investigation: Official Journal of the Italian Society of Endocrinology >Circulating endogenous digitalis-like factor(s) (EDLF) in man is derived from the adrenals and its secretion is ACTH-dependent.
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Circulating endogenous digitalis-like factor(s) (EDLF) in man is derived from the adrenals and its secretion is ACTH-dependent.

机译:人的循环内源性洋地黄样因子(EDLF)来自肾上腺,其分泌是ACTH依赖性的。

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Adrenal origin and ACTH-dependent secretion of endogenous digitalis-like factor(s) (EDLF) was investigated. Twelve normal weight normotensive subjects (normal group) and 10 patients with Addison's disease (Addison group) were subjected to prolonged ACTH stimulation with 1 mg tetracosactin-depot im. Blood sampling was at 0 and 240 min. Digitalis-like reactivity was monitored in plasma extracts (combined organic solvent solid phase method) by digoxin and ouabain radioimmunoassay (RIAD and RIAO, respectively). 3H-ouabain concentration on erythrocytes (OBS) was also determined. Na+, K+-ATPase inhibition by normal plasma extract was tested by measuring Vmax and Km of 86Rb+-transport into human erythrocytes. In the normal group basal median plasma concentrations RIAD (0.07 nmol/l) and RIAO (0.89 nmol/l) increased significantly after ACTH administration (median 0.31 and 1.83, respectively; Wilcoxon, p<0.01). In contrast, in the Addison group no plasma RIAD and RIAO reactivity was detected before or after ACTHadministration with minor exceptions. The OBS remained unchanged in the Addison group at 0 and 240 min; in the normal group there was a significant decline at 240 min (Wilcoxon, p<0.05) implying increase in circulating EDLF after ACTH stimulation. In the 86Rb+-transport experiments, 2 nmol/l ouabain or 2 nmol/l plasma-extracted ouabain reactivity both significantly impaired substrate affinity equally increasing Km without affecting Vmax. In men, the adrenals may produce and secrete EDLF, whose secretion appears to be ACTH-dependent.
机译:研究了内源性洋地黄样因子(EDLF)的肾上腺起源和ACTH依赖性分泌。对12名正常体重正常血压受试者(正常组)和10名艾迪生氏病患者(艾迪生组)进行长期ACTH刺激,同时给予1 mg十四酸肌钙蛋白-im。在0和240分钟时采血。通过地高辛和哇巴因放射免疫分析法(分别为RIAD和RIAO)监测血浆提取物中的洋地黄样反应性(有机溶剂固相混合法)。还确定了红细胞(OBS)上的3H-哇巴因浓度。通过测量86Rb +转运至人红细胞的Vmax和Km来测试正常血浆提取物对Na +,K + -ATPase的抑制作用。在正常组中,ACTH给药后,RIAD(0.07 nmol / l)和RIAO(0.89 nmol / l)的基础血浆中位数浓度显着增加(分别为中位数0.31和1.83; Wilcoxon,p <0.01)。相反,在Addison组中,除少数例外,在ACTH给药之前或之后均未检测到血浆RIAD和RIAO反应性。在0和240分钟时,Addison组的OBS保持不变;正常组在240分钟时有明显下降(Wilcoxon,p <0.05),这表明ACTH刺激后循环EDLF增加。在86Rb +转运实验中,2 nmol / l的哇巴因或2 nmol / l的血浆提取的哇巴因反应性均显着削弱了底物亲和力,同样增加了Km而不影响Vmax。在男性中,肾上腺可能产生并分泌EDLF,EDLF的分泌似乎是ACTH依赖性的。

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